The Recall Desk

State

Colorado product recalls

20,322 recalls have nationwide distribution and so reach Colorado. 0 additional recalls listed Colorado specifically in their distribution scope.

About recalls in Colorado

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Colorado consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

12851–12875 of 20322

  • SevereCPSC·23229·2023-06-22

    Zuru Recalls 7.5 Million Baby Shark Bath Toys for Impalement Risk

    Zuru is recalling about 7.5 million Robo Alive Junior Baby Shark bath toys due to hard plastic top fins that pose risks of impalement, laceration, and puncture injuries to children. Twelve reported injuries have been documented, including nine cases requiring stitches or medical attention.

    Product
    Robo Alive Junior Baby Shark Sing & Swim Bath Toys (full-size) and Robo Alive Junior Mini Baby Shark Swimming Bath Toys (mini-size)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·23231·2023-06-22

    Research Products Steam Humidifiers Recalled for Fire Hazard

    Research Products is recalling about 36,200 steam humidifiers with faulty electrode connector wires that can loosen, cause arcing, and overheat. The company has received 103 reports of overheating, including 10 residential fires causing over $10 million in damage.

    Product
    Steam Humidifiers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23227·2023-06-22

    Iron Dietary Supplements Recalled Due to Non-Child-Resistant Packaging

    Nationwide Pharmaceutical is recalling Ferrous Sulfate enteric-coated tablets because the packaging does not meet child-resistant requirements, posing a poisoning risk to young children. About 4,000 bottles were sold at major retailers from December 2022 through January 2023.

    Product
    Ferrous Sulfate (Iron) Enteric-Coated Tablets, 324 mg - 100 Tablet Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23770·2023-06-22

    Infanttech Zooby Video Baby Monitors Recalled for Fire Hazard

    Infanttech is recalling about 17,100 Zooby video baby monitors for cars because the battery can malfunction, overheat, and burst, posing a fire hazard. The company has received three reports of the monitors catching fire, with no injuries reported.

    Product
    Zooby video baby monitors for cars
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23230·2023-06-22

    Hurtle Multi-Purpose Helmets Recalled Due to Risk of Head Injury

    Sound Around is recalling about 1,800 Hurtle multi-purpose children's helmets because they do not meet federal safety standards for positional stability and may fail to protect in a crash.

    Product
    Hurtle Multi-Purpose Helmet
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23228·2023-06-22

    Boost The Mood Ceramic Mugs Recalled Due to Fire Hazard

    Ceramic mugs labeled "microwave safe" can spark and catch fire when microwaved due to metallic print. About 26,400 units were sold at Ulta Beauty stores and online from October 2022 through March 2023.

    Product
    Boost The Mood Ceramic Mugs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23769·2023-06-22

    Havertys Concord Dual Power Recliner Chairs Fall Hazard Recall

    About 930 Havertys Concord Dual Power Recliner Chairs are being recalled because the chair back can detach during use, posing a fall hazard. The firm has received nine reports of detachment, including two with reported injuries to the back, neck, and hip.

    Product
    Havertys Concord Dual Power Recliner Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23226·2023-06-22

    Poseidon M28A Dive Computers Recalled Due to Water Intake Hazard

    Poseidon M28A Dive Computers can stop working when water enters the device, causing the depth sensor to malfunction and loss of dive data. The firm has received one report of water intake but no injuries have been reported.

    Product
    Poseidon M28A Dive Computers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0874-2023·2023-06-21

    Hand sanitizer recalled nationwide for methanol contamination

    SOFT HANDS Alcohol Antiseptic 80% hand sanitizer is recalled nationwide due to FDA detection of methanol contamination. Approximately 7,303 gallons were distributed with manufacture dates from March to August 2020.

    Product
    SOFT HANDS Alcohol Antiseptic 80%, Topical Solution, HAND SANITIZER, NON-STERILE SOLUTION, cleanpro SUPPLY, 1 US gallon / 3785.41ml, plastic gallon bottle, MCS Midwest Cleaning Solutions, 404 Noid Rd., Canton, SD 57013.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0873-2023·2023-06-21

    Hand Sanitizer Containing Methanol Recalled Due to Chemical Contamination

    Jarman's Midwest Cleaning Systems recalled 2,365 gallons of 80% alcohol antiseptic hand sanitizer nationwide due to FDA-detected methanol contamination. Consumers should stop using affected products immediately.

    Product
    Alcohol Antiseptic 80%, Topical Solution, Hand Sanitizer, Non-sterile Solution, Volume: 3.785 L, plastic gallon bottle, MCS Midwest Cleaning Solutions, 404 Noid Rd., Canton, SD 57013.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1667-2023·2023-06-21

    Nitric Oxide Delivery System check valve misalignment risk

    NOxBOXi Nitric Oxide Delivery System devices may malfunction due to misaligned check valves, risking gas leaks and therapy interruption. This could lead to oxygen desaturation if the device fails during patient use.

    Product
    NOxBOXi Nitric Oxide Delivery System, NOXBOX-I, REQNOXBOX-I, Nitric Oxide Delivery Device
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0988-2023·2023-06-21

    Hu Vanilla Crunch Dark Chocolate recalled for undeclared tree nuts

    HU PRODUCTS is recalling Hu Vanilla Crunch Dark Chocolate bars nationwide because they may contain undeclared tree nuts, which pose a risk to consumers with tree-nut allergies.

    Product
    Hu Vanilla Crunch Dark Chocolate bar
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1920-2023·2023-06-21

    Aspira Drainage Catheter Insertion Tray valve assembly may fail to open

    Merit Medical Systems is recalling certain Aspira Drainage Catheter Insertion Trays (Model 15.5F) due to a potential valve assembly defect that could prevent fluid drainage. No injuries have been reported.

    Product
    Aspira Drainage Catheter Insertion Tray 15.5F, REF: ASP-15-5, STERILE EO, Rx Only *EU Distribution only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1915-2023·2023-06-21

    Aspira Pleural Drainage Catheter Insertion Tray recalled due to valve failure

    Merit Medical Systems recalls the Aspira Pleural Drainage Catheter Insertion Tray due to a potential valve failure that could prevent fluid drainage. The recall affects approximately 1054 units distributed nationwide and internationally.

    Product
    Aspira Pleural Drainage Catheter Insertion Tray 15.5F, REF: 4992509, Version A, Sterile EO, Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1916-2023·2023-06-21

    Aspira Valve Repair Kit may fail to open and obstruct fluid drainage

    Merit Medical Systems is recalling Aspira Valve Repair Kits because valve assemblies may fail to open, preventing fluid drainage. The FDA Class II recall affects 2,559 units distributed across the US and internationally.

    Product
    Aspira Valve Repair Kit, REF: 4992306 Version A, Sterile EO, Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1912-2023·2023-06-21

    Aspira Pleural Drainage Catheter Insertion Tray recalled for valve assembly malfunction

    Merit Medical Systems is recalling the Aspira Pleural Drainage Catheter Insertion Tray because valve assemblies may not open, preventing proper fluid drainage.

    Product
    Aspira Pleural Drainage Catheter Insertion Tray 15.5F, REF 4992506, Version A, Sterile EO, Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1917-2023·2023-06-21

    Aspira Drainage Catheter Insertion Tray May Have Non-Opening Valve

    Merit Medical Systems recalls Aspira Drainage Catheter Insertion Trays due to potential valve assembly malfunction that could prevent fluid drainage.

    Product
    Aspira Drainage Catheter Insertion Tray 15.5F, REF: ASP-11, STERILE EO, Rx Only *EU Distribution only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1825-2023·2023-06-21

    Philips Tempus LS-Manual Defibrillator pacing failure due to communication error

    A communication failure in the Philips Tempus LS-Manual Defibrillator may prevent pacing delivery. The device displays an error message and potentially becomes ineffective, affecting approximately 1,147 units distributed nationwide.

    Product
    Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1968-2023·2023-06-21

    Tearaway Introducer Kit Recalled Due to Potential Connector Defect

    Galt Medical Corporation is recalling Tearaway Introducer Kits due to potential cracking or dislodging of the luer connection during use, which can render the device unusable and require replacement.

    Product
    Tearaway Introducer Kit, REF: KIT-010-12, KIT-010-17, KIT-900-16
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1919-2023·2023-06-21

    Aspira Drainage Catheter Insertion Tray recalled due to valve malfunction

    Merit Medical Systems is recalling Aspira Drainage Catheter Insertion Tray 15.5F due to potential valve assembly failure that may prevent fluid drainage. No injuries reported.

    Product
    Aspira Drainage Catheter Insertion Tray 15.5F, REF: ASP-15, STERILE EO, Rx Only *EU Distribution only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1913-2023·2023-06-21

    Aspira Pleural Drainage Catheter May Fail to Drain Fluid

    Merit Medical Systems is recalling 524 units of the Aspira Pleural Drainage Catheter Insertion Tray due to a defect where valve assemblies may not open, preventing fluid drainage. Affected units were distributed worldwide including across the US, France, UK, and Mexico.

    Product
    Aspira Pleural Drainage Catheter Insertion Tray 15.5F, REF 4992507, Version A, Sterile EO, Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1703-2023·2023-06-21

    Medicine Dropper Recalled for Potential Glass Particulate Contamination

    Apothecary Products, LLC is recalling 1,596 units of Medicine Dropper (Lot 021623) due to potential glass particles on the dropper bulb exterior. Glass particles could contaminate medication or cause injury.

    Product
    Medicine Dropper, Product Code K508
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1702-2023·2023-06-21

    Eye and Ear Dropper Recalled for Potential Glass Particulate Contamination

    Apothecary Products is recalling Eye and Ear Droppers (Product Code 67082) due to the potential for glass particulate on the dropper bulb's external surface. Consumers should stop using affected units immediately.

    Product
    Eye and Ear Dropper, Product Code 67082
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1966-2023·2023-06-21

    bellavista 1000 Ventilator Recalled for Software Hang and Use Error Risk

    Vyaire Medical is recalling approximately 910 units of the bellavista 1000 Ventilator due to a software issue that can cause the touchscreen to become unresponsive and a potential use error risk if operators do not confirm settings are appropriate for the patient.

    Product
    bellavista 1000 Ventilator, Catalogue Number 301.100.030; Continuous Use Ventilator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1910-2023·2023-06-21

    Aspira Peritoneal Drainage Catheter Insertion Tray valve malfunction

    Merit Medical's Aspira Peritoneal Drainage Catheter Insertion Tray valve assemblies may fail to open, preventing fluid drainage. 175 units distributed nationwide and internationally are affected.

    Product
    Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F, REF 4992208 Version A, Sterile EO, Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide